Fenchol (BioDeep_00000004901)

 

Secondary id: BioDeep_00000228620, BioDeep_00000265838, BioDeep_00000638392, BioDeep_00001868661

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-, (1R-endo)-

化学式: C10H18O (154.1357578)
中文名称: 溶剂红172, 小茴香醇, 葑醇
谱图信息: 最多检出来源 Viridiplantae(plant) 0.21%

分子结构信息

SMILES: CC1(C)C2CCC(C)(C2)C1O
InChI: InChI=1S/C10H18O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7-8,11H,4-6H2,1-3H3

描述信息

Fenchol is found in fennel. Fenchol is a flavouring ingredient with a bitter, lime-like flavour [DFC] (Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.).
Fenchol is a natural product found in Kunzea salina, Hyptis goyazensis, and other organisms with data available.
Flavouring ingredient with a bitter, lime-like flavour [DFC]
Fenchyl alcohol is a monoterpene alcohol in the essential oils isolated from Douglas fir needles, acts as a fragrance. Fenchyl alcohol strongly inhibits the rumen microbial activity of both sheep and deer[1][2].
Fenchyl alcohol is a monoterpene alcohol in the essential oils isolated from Douglas fir needles, acts as a fragrance. Fenchyl alcohol strongly inhibits the rumen microbial activity of both sheep and deer[1][2].

同义名列表

36 个代谢物同义名

Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-, (1R-endo)-; (1S,2S,4R)-1,3,3-Trimethyl-bicyclo[2.2.1]heptan-2-ol; (1S,2R,4R)-1,3,3-TRIMETHYL-BICYCLO[2.2.1]HEPTAN-2-OL; Bicyclo(2.2.1)heptan-2-ol, 1,3,3-trimethyl-; Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-; 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol #; 2,2,4-trimethylbicyclo[2.2.1]heptan-3-ol; 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol; 1,3,3-Trimethylbicyclo(2.2.1)heptan-2-ol; 3,3-Dimethyl-8,9-dinorbornan-2-ol; 2-Norbornanol, 1,3,3-trimethyl-; 1,3,3-trimethyl-2-norbornanol; fenchol, ((endo)-(+-))-isomer; fenchol, ((exo)-(+-))-isomer; 1,3,3-Trimethyl-2-norborneol; fenchol, (1S-endo)-isomer; fenchol, (1R-endo)-isomer; fenchol, (1S-exo)-isomer; fenchol, (endo)-isomer; fenchol, (exo)-isomer; FENCHYL ALCOHOL (OD); fenchylic alcohol; (-)-alpha-fenchol; .alpha.-Fenchol; Fenchyl alcohol; Fenchol, exo-; alpha-Fenchol; endo-fenchol; Tox21_303498; (+)-Fenchol; SMP2_000026; 2-Fenchanol; FEMA 2480; AI3-00733; Fenchol; (-)-endo-Fenchol



数据库引用编号

23 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(2)

代谢反应

3 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(3)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

68 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。



文献列表

  • Mohamed Salim, T K Ahmedul Kabeer, S Ajikumaran Nair, Mathew Dan, M Sabu, Sabulal Baby. Chemical profile, antiproliferative and antioxidant activities of rhizome oil of Zingiber anamalayanum from Western Ghats in India. Natural product research. 2016 Sep; 30(17):1965-8. doi: 10.1080/14786419.2015.1094802. [PMID: 26456637]
  • Maria Graça Miguel, Maria Dulce Antunes. Is propolis safe as an alternative medicine?. Journal of pharmacy & bioallied sciences. 2011 Oct; 3(4):479-95. doi: 10.4103/0975-7406.90101. [PMID: 22219581]
  • Ameur Elaissi, Hanène Medini, Mohamed Larbi Khouja, Monique Simmonds, Frederic Lynen, Farhat Farhat, Rachid Chemli, Fethia Harzallah-Skhiri. Variation in volatile leaf oils of five Eucalyptus species harvested from Jbel Abderrahman arboreta (Tunisia). Chemistry & biodiversity. 2011 Feb; 8(2):352-61. doi: 10.1002/cbdv.201000102. [PMID: 21337507]
  • Habib Abbasipour, Mohammad Mahmoudvand, Fahimeh Rastegar, Mohammad Hossein Hosseinpour. Fumigant toxicity and oviposition deterrency of the essential oil from cardamom, Elettaria cardamomum, against three stored–product insects. Journal of insect science (Online). 2011; 11(?):165. doi: 10.1673/031.011.16501. [PMID: 22242564]
  • Rajendra C Padalia, Ram S Verma, Velusamy Sundaresan, Chandan S Chanotiya. Chemical diversity in the genus Alpinia (Zingiberaceae): comparative composition of four Alpinia species grown in Northern India. Chemistry & biodiversity. 2010 Aug; 7(8):2076-87. doi: 10.1002/cbdv.201000013. [PMID: 20730971]
  • Rajendra C Padalia, Chandan S Chanotiya, V Sundaresan. Compositional variability in essential oil from different parts of Alpinia speciosa from India. Natural product communications. 2010 Feb; 5(2):279-82. doi: . [PMID: 20334144]
  • Recep Kotan, Saban Kordali, Ahmet Cakir. Screening of antibacterial activities of twenty-one oxygenated monoterpenes. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2007 Jul; 62(7-8):507-13. doi: 10.1515/znc-2007-7-808. [PMID: 17913064]
  • A Wajs, A Pranovich, M Reunanen, S Willför, B Holmbom. Characterisation of volatile organic compounds in stemwood using solid-phase microextraction. Phytochemical analysis : PCA. 2006 Mar; 17(2):91-101. doi: 10.1002/pca.891. [PMID: 16634285]
  • D Yang, F Wang, J Peng, S Ren. [GC-MS analysis and inhibitory activity of the essential oil extracted from the leaves of Lindera communis]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 1999 Mar; 22(3):128-31. doi: ". [PMID: 12575094]